A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501227



Internal ID22559165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129560283..129565410hg38UCSC Ensembl
chr7:129200124..129205251hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg385128
hg195128
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501227
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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